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Senior Clinical Trials Manager
ImmunityBio, Inc.Manage global clinical studies, developing protocols and training clinical site staff for a biotechnology company. Provide ongoing support and guidance to ensure compliance and safety in clinical trials.
Posted 5/23/2026full-timeRemote • California • 🇺🇸 United StatesSenior💰 $143,000 - $165,000 per yearWebsite
About the role
Key responsibilities & impact- Responsible for managing the activities of several global clinical studies
- Assist in the development of study-related documents, study site management, and patient data monitoring
- Provide guidance to clinical sites on a daily basis including protocol interpretation and protocol safety compliance
- Lead in reviewing completed assignments by members of the clinical development group
- Lead/assist in the development and management of revisions to study-related documents such as the informed consent, laboratory manual, pharmacy manual, case report forms (CRFs) and other study execution tools
- Provide support in site recruitment, site initiation, site payments and site close-out
- Help to oversee the training of new clinical site staff or site training for protocol amendments
- Liaise with the in-house team to ensure collection of updated regulatory documents as needed
- Help to provide guidance to clinical sites on a daily basis including protocol interpretation and protocol safety compliance
- Lead/Assist in the training of clinical development group staff
- Assist CPM to prepare and update clinical trial updates for Clinical Development team
- Provide support for summarizing and maintaining patient treatment, response and survival data for active studies
Requirements
What you’ll need- Bachelor’s degree with 7+ years of relevant experience in clinical research required
- Proficiency in MS Word, Excel, PowerPoint, Outlook
- Excellent written/oral communication skills as well as strong organizational and multi-tasking skills.
- Understand the job-specific system and processes as defined by the company’s SOPs and adhere to the requirements listed in those documents.
Benefits
Comp & perks- Medical, Dental and Vision Plan Options
- Health and Financial Wellness Programs
- Employer Assistance Program (EAP)
- Company Paid and Voluntary Life/AD&D, Short-Term and Long-Term Disability
- Healthcare and Dependent Care Flexible Spending Accounts
- 401(k) Retirement Plan with Company Match
- 529 Education Savings Program
- Voluntary Legal Services, Identity Theft Protection, Pet Insurance and Employee Discounts, Rewards and Perks
- Paid Time Off (PTO) includes: 11 Holidays
- Exempt Employees are eligible for Unlimited PTO
- Non-Exempt Employees are eligible for 10 Vacation Days, 56 Hours of Health Pay, 2 Personal Days and 1 Cultural Day
ATS Keywords
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Hard Skills & Tools
clinical study managementprotocol interpretationpatient data monitoringstudy-related document developmentsite recruitmentsite initiationsite close-outtraining of clinical site staffclinical trial updatesdata summarization
Soft Skills
written communicationoral communicationorganizational skillsmulti-tasking skillsleadershipguidancecollaboration